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Helium Oxygen

HELIUM OXYGEN LABEL 70 30

Approved
Approval ID

d43bccaa-d16a-4c2d-8810-cfa1b74b2e37

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 18, 2010

Manufacturers
FDA

Airgas National Welders

DUNS: 003162310

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Helium Oxygen

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code11896-0018
Product Classification
G
Generic Name
Helium Oxygen
Product Specifications
Route of AdministrationRESPIRATORY (INHALATION)
Effective DateOctober 18, 2010
FDA Product Classification

INGREDIENTS (2)

HeliumActive
Quantity: 700 mL in 1 L
Code: 206GF3GB41
Classification: ACTIB
OxygenActive
Quantity: 300 mL in 1 L
Code: S88TT14065
Classification: ACTIB

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Helium Oxygen - FDA Drug Approval Details